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乳腺癌组织中DNA修复酶MGMT、XRCC1的表达与临床预后因素的关系 被引量:7

DNA repair enzymes O6-methylguanine-DNA methytransferase and X-ray repair cross complementing 1 and the clinical prognostic factors in breast cancer
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摘要 目的 探讨乳腺癌组织中O6-甲基鸟嘌呤-DNA-甲基转移酶(MGMT)和X线修复交叉互补基因1(XRCC1)的表达及与临床预后因素的关系.方法 采用SP免疫组织化学法检测110例乳腺癌石蜡标本、19例纤维腺瘤石蜡标本及11例正常乳腺组织石蜡标本中MGMT和XRCC1蛋白的表达,分析其与临床预后因素的关系.结果 110例乳腺癌组织中MGMT阳性表达率为71.8%,其表达与乳腺癌患者的病理类型、浸润性导管癌的病理分化程度、淋巴结是否转移及ER表达明显相关(P<0.05).XRCC1阳性表达率为30.9%,其表达与患者的肿瘤大小、浸润性导管癌的病理分化程度明显相关(P<0.05).此外,MGMT与XRCC1的表达明显相关(P<0.05),生存分析表明MGMT、XRCC1是影响生存期的因素(P<0.05).结论 DNA修复基因MCMT及XRCC1是临床评估乳腺癌恶性程度、判断预后及制定治疗策略的病理指标之一. Objective To investigate the expression of O6-methylguanine-DNA methytransferase (MGMT) and X-ray repair cross complementing 1 (XRCC1) in breast cancer, and their relationship with clinical prognostic factors. Methods Immunohistochemistry (S-P) was performed for MGMT and XRCC1 on 110 specimens of breast cancer, 19 specimens of fibroadenoma and 11 specimens of normal breast tissues. Results The positive expression rate of MGMT was 71.8%, which had a correlation with pathological classification, pathological grades of infitrating ductal carcinoma ( IDG), axillas lymph nodes metastasis, and expression of ER ( P 〈 0.05). The positive expression rate of XRCC1 was 30.9%, which had a correlation with the tumor size and the pathological grades of IDG. The expression rate of MGMT had a positive correlation with XRCC1 (P 〈0.05). The survival analysis showed that MGMT and XRCC1 may be considered a independent maker in breast cancer ( P 〈 0.05 ). Conclusion MGMT and XRCC1 were important pathological signs to evaluate the malignancy degree and prognosis of the breast cancer. These markers play an important role in working out the treatment prescription for breast cancer patients.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2010年第10期1418-1421,共4页 Chinese Journal of Experimental Surgery
基金 基金项目:黑龙江省科技攻关计划资助项目(GB08C401-01)
关键词 乳腺癌 预后 免疫组织化学 Breast cancer Prognosis Immunohistochemistry
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参考文献13

  • 1Christmann M,Tomicic MT,Roos WP,et al.Mechanisms of human DNA repair:an update.Toxicology,2003,193:3-34.
  • 2朱凌冬,蔡景龙,远里美.O^6-甲基鸟嘌呤-DNA-甲基转移酶的研究进展[J].肿瘤防治研究,2005,32(12):802-804. 被引量:11
  • 3Thacker J,Zdzienicka MZ.The mammalian XRCC genes:their roles in DNA repair and genetic stability.DNA Repair,2003,2:655-672.
  • 4付强,于世英,许三鹏.乳腺癌HER2过度表达预后相关因素研究[J].肿瘤防治研究,2008,35(S1):9-11. 被引量:8
  • 5王深明.乳腺外科实验研究的发展方向[J].中华实验外科杂志,2006,23(5):519-521. 被引量:5
  • 6Kokkinakis DM,Ahmed MM,Delgade R,et al.Role of O6-methylgulanine-DNA methyltransferase in the resistance of parcreartic tumors to DNA alkylating agents.Cancer Res,1997,57:53-60.
  • 7Wood RD,Mitchell M,Sgouros J,et al.Human DNA repair genes.Science,2001,11:1513-1530.
  • 8Citron M,Schoenhaus M,Rothenberg H,et al.O6-methylguanine-DNA alkyltransferase gene is elevated in malignant tissue of the breast.Cancer Invest,1994,12:605-610.
  • 9崔灵芝,宋三泰,江泽飞,章杨培,李晓兵,李素波.MGMT蛋白的表达与乳腺癌预后关系初探[J].肿瘤研究与临床,2004,16(2):88-90. 被引量:3
  • 10Anne C,Frederique P,Monique D.O6-Methylguanine-DNA gene expression and prognosis in breast carcinoma.International Journal of Oncology,2002,21:1125-1131.

二级参考文献40

  • 1杨军,阵建敏,章扬培.O^6-甲基鸟嘌呤DNA甲基转移酶基因表达提高肿瘤细胞的烷化抗性[J].科学通报,1996,41(3):252-255. 被引量:4
  • 2萨姆布鲁克J 弗里奇E F 曼尼阿蒂斯T 黄培堂 王嘉玺 朱厚础 等.分子克隆实验指南 第3版[M].北京:科学出版社,2002..
  • 3Hulka BS. Epidemiologic analysis of breast and gynecologic cancers. Prog Clin Biol Res, 1997,396 : 17-29.
  • 4Kristensen VN, Borresen-Dale AL. Molecular epidemiology of breast cancer: genetic variation in steroid hormone metabolism. Mutat Res, 2000,462:323-333.
  • 5Long JR, Kataoka N, Shu XO, et al. Genetic polymorphisms of the CYP19A1 gene and breast cancer survival. Cancer Epidemiol Biomarkers Prey,2006,15 : 2115 -2122.
  • 6Haiman CA, Dossus L, Setiaman VW, et al. Genetic variation at the CYP19A1 locus predicts circulating estrogen levels but not breast cancer risk in postmenopausal women. Cancer Res, 2007, 67 : 1893-1897.
  • 7Haiman CA, Stram DO, Pike MC, et al. A comprehensive haplotype analysis of CYP19 and breast cancer risk:the Multiethnic Cohort. Hum Mol Genet ,2003,12:2679-2692.
  • 8Olson JE, Ingle jN,Ma CX, et al. A comprehensive examination of CYP19 variation and risk of breast cancer using two haplotype-tagging approaches. Breast Cancer Res Treat,2007,102:237-247.
  • 9Olson JE, Ma CX, Pelleymounter LL, et al. A comprehensive examination of CYP19 variation and breast density. Cancer Epidemiol Biomarkers Prey ,2007,16:623-625.
  • 10Ma CX, Adjei AA, Salavaggione OE, et al. Human aromatase: Gene resequencing and functional genomics. Cancer Res, 2005, 65: 11071-11082.

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